Grow your clinical research skills with PAREXEL FSP as a Clinical Study Administrator in Mississauga, Ontario. This hybrid role will involve supporting the entire study lifecycle from start up to completion.

In this role, you will coordinate with the Local Study Team and assist in ensuring high-quality deliverables. Your key skills in organization and administration will help manage document submissions and compliance throughout the study process. The position offers a blend of on-site and remote work, promoting flexibility while ensuring project success.

Key Responsibilities:
• Assist in clinical study coordination and administration
• Review and track application documents for submission
• Serve as the contact point for investigators and CRAs




• Ensure eTMF and ISF maintenance according to guidelines
• Track study materials and regulatory documents

Requirements:
• Secondary school qualifications relevant to the role
• Previous administrative experience, preferably in life sciences
• Solid organizational skills and attention to detail
• Good command of English for effective communication
• Ability to multitask in a fast-paced environment

Join PAREXEL FSP to make a meaningful difference in clinical research through effective study administration and coordination.
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📌 PAREXEL FSP Clinical Study Administrator (Ontario)
🏢 Parexel International
📍 Ontario